2-(Morpholinomethyl)-1-phenyl-hex-5-yn-1-one

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Identification

Molecular formula
C17H21NO2
CAS Number
87691-87-0
IUPAC Name
2-(morpholinomethyl)-1-phenyl-hex-5-yn-1-one
Molecular Weight
243.32g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1743g/cm3
Interesting facts

Interesting Facts about 2-(Morpholinomethyl)-1-phenyl-hex-5-yn-1-one

2-(Morpholinomethyl)-1-phenyl-hex-5-yn-1-one is an intriguing compound that highlights the fascinating intersections between organic chemistry and medicinal research. Here are some key points to consider:

  • Structural Richness: The compound features a unique hex-5-yn-1-one structure, incorporating both alkyne and ketone functionalities, which offers a variety of sites for potential chemical reactivity. Such complex structures can lead to the discovery of new chemical properties and behaviors.
  • Role of Morpholine: The morpholino group attached to the compound plays a pivotal role in influencing its biological activity. Morpholine rings are often found in pharmacologically active compounds and can enhance solubility and selectivity in biological systems.
  • Potential Applications: Given its structure, this compound is of great interest in medicinal chemistry and drug development. Researchers are exploring its potential as a lead compound for the synthesis of novel therapeutics targeting various diseases.
  • Reactivity Insights: The alkyne moiety opens avenues for further modifications through coupling reactions, allowing chemists to create an array of derivatives with varying biological activities.
  • Research Tool: The compound can be utilized in synthetic organic pathways to develop more complex molecules, showcasing its value as a versatile building block in chemical synthesis.

In the words of a renowned chemist, "The beauty of chemistry lies in its ability to transform simple building blocks into complex, functional molecules." The exploration of 2-(morpholinomethyl)-1-phenyl-hex-5-yn-1-one exemplifies this principle, reflecting both the creativity and precision of chemical science.

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